Key Documents

View All Documentation

B34729

Biphenyl-4-carboxylic acid

Name: Biphenyl-4-carboxylic acid
Brand: ALDRICH

95%

Synonym(s):

4-Phenylbenzoic acid

Select a Size

Change View

About This Item

Linear Formula:

C₆H₅C₆H₄CO₂H

CAS Number:

92-92-2

Molecular Weight:

198.22

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24891723

EC Number:

202-203-1

Beilstein/REAXYS Number:

973519

MDL number:

MFCD00002553

Assay:

95%

Form:

crystals

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

100

assay

95%

form

crystals

mp

220-225 °C (lit.)

SMILES string

OC(=O)c1ccc(cc1)-c2ccccc2

InChI

1S/C13H10O2/c14-13(15)12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H,(H,14,15)

InChI key

NNJMFJSKMRYHSR-UHFFFAOYSA-N

Gene Information

human ... ALB(213), BAD(572)

Description

pictograms

GHS07

signalword

Warning

hcodes

H319

pcodes

P264 - P280 - P305 + P351 + P338 - P337 + P313

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Molecular transport in ionic liquid/nanomembrane hybrids.

Daniil Naberezhnyi et al.

Physical chemistry chemical physics : PCCP, 22(17), 9808-9814 (2020-04-28)

Ionic liquids and nanoscale membranes are both considered as promising functional components to design next-generation gas separation technologies. Herein, we combine free-standing carbon nanomembranes (CNMs) with [bmim][Tf2N] ionic liquid having affinity to carbon dioxide, and explore molecular permeation through such

Studies on the absorption mechanism for the glucuronide of p-phenyl benzoic acid in fetal compartment.

T Nanbo

Journal of pharmacobio-dynamics, 5(12), 988-993 (1982-12-01)

The mechanism responsible for the deconjugation of the glucuronide of p-phenyl benzoic acid (PPBA) in fetal intestine and amniotic fluid was studied in rats. Non-enzymatic hydrolysis of PPBA glucuronide in intestine was little before birth. The activity of beta-glucuronidase (beta-G)

Change in kinetic properties and metabolic clearance of UDP-glucuronyltransferase for p-phenyl benzoic acid in developing fetus of rat.